Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5279652 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Bouillomides A (1) and B (2) are two depsipeptide analogues of dolastatin 13. Isolated from a Guamanian sample of Lyngbya bouillonii, the planar structures were elucidated on the basis of HR-ESI-MS and NMR data, while the absolute configurations were determined by employing functional group conversions, modified Marfey's analysis, and detailed analyses of ROESY correlations. Compounds 1 and 2 selectively inhibited serine proteases elastase (IC50 = 1.9 μM for both) and chymotrypsin (IC50 = 0.17 and 9.3 μM, respectively) while showing no inhibition of trypsin (IC50 >100 μM).
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Brent K. Rubio, Stephen M. Parrish, Wesley Yoshida, Peter J. Schupp, Tom Schils, Philip G. Williams,